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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Gorlin Syndrome: Recent Advances in Genetic Testing and Molecular and Cellular Biological Research
Shoko Onodera, Yuriko Nakamura, Toshifumi Azuma
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 20, pp. 7559-7559
Open Access | Times Cited: 55

Showing 1-25 of 55 citing articles:

Hedgehog signaling in tissue homeostasis, cancers, and targeted therapies
Junjun Jing, Zhuoxuan Wu, Jiahe Wang, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 79
Ultraviolet Radiation Biological and Medical Implications
Tarek Al-Sadek, Nabiha Yusuf
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 3, pp. 1924-1942
Open Access | Times Cited: 18
Hereditary cancer syndromes
Evgeny N. Imyanitov, Ekatherina Sh. Kuligina, Anna P. Sokolenko, et al.
World Journal of Clinical Oncology (2023) Vol. 14, Iss. 2, pp. 40-68
Open Access | Times Cited: 30
Gorlin Syndrome-Associated Basal Cell Carcinomas Treated with Vismodegib or Sonidegib: A Retrospective Study
Giulia Murgia, Luca Valtellini, Nerina Denaro, et al.
Cancers (2024) Vol. 16, Iss. 12, pp. 2166-2166
Open Access | Times Cited: 6
Pharmacological modulation of Sonic Hedgehog signaling pathways in Angiogenesis: A mechanistic perspective
Ashi Mannan, Sonia Dhiamn, Nikhil Garg, et al.
Developmental Biology (2023) Vol. 504, pp. 58-74
Closed Access | Times Cited: 11
Dual PTCH2 mutation [Ser391*, Leu104Pro]: unveiling a potential new genetic susceptibility factor for glioma development
Xiang Li, Yingting Wu, Tiantian Han, et al.
Investigational New Drugs (2025)
Closed Access
Clinical Features and PTCH1 Expression in Gorlin–Goltz Syndrome: A Case Report
Gabriela González-López, Sergio Alberto Mendoza-Álvarez, Claudia Patricia Mejía-Velázquez, et al.
Reports — Medical Cases Images and Videos (2025) Vol. 8, Iss. 1, pp. 34-34
Open Access
Navigating Beyond a Cyst: The Intricate World of Gorlin Goltz Syndrome - A Case Report
Aksha Bhargava, Vikas Kunwar Singh, Ruchika Tiwari, et al.
Annals of Maxillofacial Surgery (2025)
Closed Access
Basal Cell Nevus Syndrome and Sporadic Basal Cell Carcinoma: A Comparative Study of Clinicopathological Features
Ching-Ya Wang, Chun-Bing Chen, Franchesca Marie D. Ilagan, et al.
Acta Dermato Venereologica (2025) Vol. 105, pp. adv40692-adv40692
Open Access
Cholesterol and Hedgehog Signaling: Mutual Regulation and Beyond
Shouying Xu, Chao Tang
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 16
Basal cell nevus syndrome: an update on clinical findings
Lucía T. Fernández, Sonia Sofìa Ocampo‐Garza, Guillermo Elizondo‐Riojas, et al.
International Journal of Dermatology (2021) Vol. 61, Iss. 9, pp. 1047-1055
Closed Access | Times Cited: 19
Oral and Maxillo-Facial Manifestations of Systemic Diseases: An Overview
Saverio Capodiferro, Luisa Limongelli, Gianfranco Favia
Medicina (2021) Vol. 57, Iss. 3, pp. 271-271
Open Access | Times Cited: 18
The Emerging Role of Hedgehog Signaling in Viral Infections
Yulin Zhou, Jinhua Huang, Boxin Jin, et al.
Frontiers in Microbiology (2022) Vol. 13
Open Access | Times Cited: 11
PTCH2 is not a strong candidate gene for gorlin syndrome predisposition
Miriam J. Smith, D. Gareth Evans
Familial Cancer (2021) Vol. 21, Iss. 3, pp. 343-346
Open Access | Times Cited: 14
Gorlin Syndrome: Assessing Genotype-Phenotype Correlations and Analysis of Early Clinical Characteristics as Risk Factors for Disease Severity
Nicolas J. Betancourt, Mollie F. Qian, Jean R. Pickford, et al.
Journal of Clinical Oncology (2022) Vol. 40, Iss. 19, pp. 2119-2127
Closed Access | Times Cited: 9
Sustained Suppression of Gorlin Syndrome-Associated Basal Cell Carcinomas with Vismodegib or Sonidegib: A Case Series
Raquel Wescott, Wolfram E. Samlowski
Current Oncology (2023) Vol. 30, Iss. 10, pp. 9156-9167
Open Access | Times Cited: 5
Modeling human cancer predisposition syndromes using CRISPR/Cas9 in human cell line models
Garrett M. Draper, Daniel J. Panken, David A. Largaespada
Genes Chromosomes and Cancer (2023) Vol. 62, Iss. 9, pp. 493-500
Open Access | Times Cited: 4
Gorlin-Goltz syndrome- report of a case with review of literature
Snehanjan Sarangi, Basudev Mahato, Samir Mandal, et al.
Medical Reports (2024), pp. 100137-100137
Open Access | Times Cited: 1
Emerging role of non-coding RNAs in the regulation of Sonic Hedgehog signaling pathway
Soudeh Ghafouri‐Fard, Tayyebeh Khoshbakht, Bashdar Mahmud Hussen, et al.
Cancer Cell International (2022) Vol. 22, Iss. 1
Open Access | Times Cited: 7
Gorlin-Like Phenotype in a Young Girl With a De Novo PTCH2 Variant Mutation of Uncertain Significance
M. García García, S García-González, Clara Cabañuz, et al.
American Journal of Dermatopathology (2024) Vol. 46, Iss. 4, pp. 247-251
Closed Access | Times Cited: 1
In Silico Analysis of Genes Associated with the Pathogenesis of Odontogenic Keratocyst
Carla Monserrat Ramírez-Martínez, Itzel Legorreta-Villegas, Claudia Patricia Mejía-Velázquez, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2379-2379
Open Access | Times Cited: 1
Clinical and genetic profiling of nevoid basal cell carcinoma syndrome in Korean patients by whole-exome sequencing
Boram Kim, Man Jin Kim, Keunyoung Hur, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 8
Gorlin–Goltz Syndrome: A Case Report and Literature Review with PTCH1 Gene Sequencing
Hyo Seong Kim, Seung Heo, Kyung Sik Kim, et al.
Archives of Plastic Surgery (2023) Vol. 50, Iss. 04, pp. 384-388
Open Access | Times Cited: 3
The role of cancer predisposition syndrome in children and adolescents with very rare tumours
Daniel Orbach, Ines B. Brecht, Nadège Corradini, et al.
EJC Paediatric Oncology (2023) Vol. 2, pp. 100023-100023
Open Access | Times Cited: 3
Progress and Current Status in Hajdu-Cheney Syndrome with Focus on Novel Genetic Research
Natsuko Aida, Tatsukuni Ohno, Toshifumi Azuma
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 19, pp. 11374-11374
Open Access | Times Cited: 5
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